Canonical Allele Identifier: CA399312860

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143288298
• MyVariant Identifiers: chr17:g.37883961T>A (hg19) ; chr17:g.39727708T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727708T>A , CM000679.2:g.39727708T>A	GRCh38
NC_000017.10:g.37883961T>A , CM000679.1:g.37883961T>A	GRCh37
NC_000017.9:g.35137487T>A	NCBI36
NG_007503.1:g.44569T>A , LRG_724:g.44569T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3432T>A MANE Select	ENSP00000269571.4:p.Asp1144Glu
ENST00000269571.9:c.3432T>A	ENSP00000269571.4:p.Asp1144Glu
ENST00000406381.6:c.3342T>A	ENSP00000385185.2:p.Asp1114Glu
ENST00000445658.6:c.2604T>A	ENSP00000404047.2:p.Asp868Glu
ENST00000541774.5:c.3387T>A	ENSP00000446466.1:p.Asp1129Glu
ENST00000578373.5:c.*3222T>A	ENSP00000463427.1:n.*3222T>A
ENST00000584450.5:c.*11T>A	ENSP00000463714.1:n.*11T>A
ENST00000584601.5:c.3342T>A	ENSP00000462438.1:p.Asp1114Glu
NM_001005862.2:c.3342T>A , LRG_724t1:c.3342T>A	NP_001005862.1:p.Asp1114Glu
NM_001289936.1:c.3387T>A , LRG_724t4:c.3387T>A	NP_001276865.1:p.Asp1129Glu
NM_001289937.1:c.*11T>A	NP_001276866.1:n.*11T>A
NM_004448.3:c.3432T>A , LRG_724t2:c.3432T>A	NP_004439.2:p.Asp1144Glu
NR_110535.1:n.3756T>A
XM_024450641.1:c.3570T>A	XP_024306409.1:p.Asp1190Glu
XM_024450642.1:c.3525T>A	XP_024306410.1:p.Asp1175Glu
XM_024450643.1:c.3480T>A	XP_024306411.1:p.Asp1160Glu
NM_001005862.3:c.3342T>A	NP_001005862.1:p.Asp1114Glu
NM_001289936.2:c.3387T>A	NP_001276865.1:p.Asp1129Glu
NM_001289937.2:c.*11T>A	NP_001276866.1:n.*11T>A
NM_001382782.1:c.3342T>A	NP_001369711.1:p.Asp1114Glu
NM_001382783.1:c.3342T>A	NP_001369712.1:p.Asp1114Glu
NM_001382784.1:c.3549T>A	NP_001369713.1:p.Asp1183Glu
NM_001382785.1:c.3534T>A	NP_001369714.1:p.Asp1178Glu
NM_001382786.1:c.3513T>A	NP_001369715.1:p.Asp1171Glu
NM_001382787.1:c.3507T>A	NP_001369716.1:p.Asp1169Glu
NM_001382788.1:c.3462T>A	NP_001369717.1:p.Asp1154Glu
NM_001382789.1:c.3453T>A	NP_001369718.1:p.Asp1151Glu
NM_001382790.1:c.3429T>A	NP_001369719.1:p.Asp1143Glu
NM_001382791.1:c.3423T>A	NP_001369720.1:p.Asp1141Glu
NM_001382792.1:c.3396T>A	NP_001369721.1:p.Asp1132Glu
NM_001382793.1:c.3390T>A	NP_001369722.1:p.Asp1130Glu
NM_001382794.1:c.3390T>A	NP_001369723.1:p.Asp1130Glu
NM_001382795.1:c.3384T>A	NP_001369724.1:p.Asp1128Glu
NM_001382796.1:c.3345T>A	NP_001369725.1:p.Asp1115Glu
NM_001382797.1:c.3333T>A	NP_001369726.1:p.Asp1111Glu
NM_001382798.1:c.3276T>A	NP_001369727.1:p.Asp1092Glu
NM_001382799.1:c.3252T>A	NP_001369728.1:p.Asp1084Glu
NM_001382800.1:c.3246T>A	NP_001369729.1:p.Asp1082Glu
NM_001382801.1:c.3228T>A	NP_001369730.1:p.Asp1076Glu
NM_001382802.1:c.3174T>A	NP_001369731.1:p.Asp1058Glu
NM_001382803.1:c.*11T>A	NP_001369732.1:n.*11T>A
NM_001382804.1:c.2604T>A	NP_001369733.1:p.Asp868Glu
NM_001382805.1:c.2481T>A	NP_001369734.1:p.Asp827Glu
NM_001382806.1:c.2394T>A	NP_001369735.1:p.Asp798Glu
NM_004448.4:c.3432T>A MANE Select	NP_004439.2:p.Asp1144Glu
NR_110535.2:n.3670T>A